217 related articles for article (PubMed ID: 29472414)
1. Laminin-521 Protein Therapy for Glomerular Basement Membrane and Podocyte Abnormalities in a Model of Pierson Syndrome.
Lin MH; Miller JB; Kikkawa Y; Suleiman HY; Tryggvason K; Hodges BL; Miner JH
J Am Soc Nephrol; 2018 May; 29(5):1426-1436. PubMed ID: 29472414
[No Abstract] [Full Text] [Related]
2. Laminin β2 gene missense mutation produces endoplasmic reticulum stress in podocytes.
Chen YM; Zhou Y; Go G; Marmerstein JT; Kikkawa Y; Miner JH
J Am Soc Nephrol; 2013 Jul; 24(8):1223-33. PubMed ID: 23723427
[TBL] [Abstract][Full Text] [Related]
3. Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane.
Funk SD; Lin MH; Miner JH
Matrix Biol; 2018 Oct; 71-72():250-261. PubMed ID: 29673759
[TBL] [Abstract][Full Text] [Related]
4. Forced expression of laminin beta1 in podocytes prevents nephrotic syndrome in mice lacking laminin beta2, a model for Pierson syndrome.
Suh JH; Jarad G; VanDeVoorde RG; Miner JH
Proc Natl Acad Sci U S A; 2011 Sep; 108(37):15348-53. PubMed ID: 21876163
[TBL] [Abstract][Full Text] [Related]
5. Pathogenicity of a Human Laminin
Funk SD; Bayer RH; Malone AF; McKee KK; Yurchenco PD; Miner JH
J Am Soc Nephrol; 2018 Mar; 29(3):949-960. PubMed ID: 29263159
[TBL] [Abstract][Full Text] [Related]
6. The glomerular basement membrane as a barrier to albumin.
Suh JH; Miner JH
Nat Rev Nephrol; 2013 Aug; 9(8):470-7. PubMed ID: 23774818
[TBL] [Abstract][Full Text] [Related]
7. A missense LAMB2 mutation causes congenital nephrotic syndrome by impairing laminin secretion.
Chen YM; Kikkawa Y; Miner JH
J Am Soc Nephrol; 2011 May; 22(5):849-58. PubMed ID: 21511833
[TBL] [Abstract][Full Text] [Related]
8. Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome.
Bull KR; Mason T; Rimmer AJ; Crockford TL; Silver KL; Bouriez-Jones T; Hough TA; Chaudhry S; Roberts IS; Goodnow CC; Cornall RJ
J Pathol; 2014 May; 233(1):18-26. PubMed ID: 24293254
[TBL] [Abstract][Full Text] [Related]
9. Proteinuria precedes podocyte abnormalities inLamb2-/- mice, implicating the glomerular basement membrane as an albumin barrier.
Jarad G; Cunningham J; Shaw AS; Miner JH
J Clin Invest; 2006 Aug; 116(8):2272-9. PubMed ID: 16886065
[TBL] [Abstract][Full Text] [Related]
10. A deletion in the N-terminal polymerizing domain of laminin β2 is a new mouse model of chronic nephrotic syndrome.
Funk SD; Bayer RH; McKee KK; Okada K; Nishimune H; Yurchenco PD; Miner JH
Kidney Int; 2020 Jul; 98(1):133-146. PubMed ID: 32456966
[TBL] [Abstract][Full Text] [Related]
11. Skeletal impairment in Pierson syndrome: Is there a role for lamininβ2 in bone physiology?
Beaufils C; Farlay D; Machuca-Gayet I; Fassier A; Zenker M; Freychet C; Bonnelye E; Bertholet-Thomas A; Ranchin B; Bacchetta J
Bone; 2018 Jan; 106():187-193. PubMed ID: 29051055
[TBL] [Abstract][Full Text] [Related]
12. First Japanese case of Pierson syndrome with mutations in LAMB2.
Togawa H; Nakanishi K; Mukaiyama H; Hama T; Shima Y; Nakano M; Fujita N; Iijima K; Yoshikawa N
Pediatr Int; 2013 Apr; 55(2):229-31. PubMed ID: 23679161
[TBL] [Abstract][Full Text] [Related]
13. Pierson syndrome in an adolescent girl with nephrotic range proteinuria but a normal GFR.
Lehnhardt A; Lama A; Amann K; Matejas V; Zenker M; Kemper MJ
Pediatr Nephrol; 2012 May; 27(5):865-8. PubMed ID: 22228401
[TBL] [Abstract][Full Text] [Related]
14. Role of the podocyte (and glomerular endothelium) in building the GBM.
Abrahamson DR
Semin Nephrol; 2012 Jul; 32(4):342-9. PubMed ID: 22958488
[TBL] [Abstract][Full Text] [Related]
15. Glomerular basement membrane composition and the filtration barrier.
Miner JH
Pediatr Nephrol; 2011 Sep; 26(9):1413-7. PubMed ID: 21327778
[TBL] [Abstract][Full Text] [Related]
16. Tensin2 is important for podocyte-glomerular basement membrane interaction and integrity of the glomerular filtration barrier.
Uchio-Yamada K; Yasuda K; Monobe Y; Akagi KI; Suzuki O; Manabe N
Am J Physiol Renal Physiol; 2020 Jun; 318(6):F1520-F1530. PubMed ID: 32390516
[TBL] [Abstract][Full Text] [Related]
17. LAMB2 mutation with different phenotypes in China
.
Zhang H; Cui J; Wang F; Xiao H; Ding J; Yao Y
Clin Nephrol; 2017 Jan; 87 (2017)(1):33-38. PubMed ID: 27925579
[TBL] [Abstract][Full Text] [Related]
18. Molecular mechanisms determining severity in patients with Pierson syndrome.
Minamikawa S; Miwa S; Inagaki T; Nishiyama K; Kaito H; Ninchoji T; Yamamura T; Nagano C; Sakakibara N; Ishimori S; Hara S; Yoshikawa N; Hirano D; Harada R; Hamada R; Matsunoshita N; Nagata M; Shima Y; Nakanishi K; Nagase H; Takeda H; Morisada N; Iijima K; Nozu K
J Hum Genet; 2020 Apr; 65(4):355-362. PubMed ID: 31959872
[TBL] [Abstract][Full Text] [Related]
19. Transgenic isolation of skeletal muscle and kidney defects in laminin beta2 mutant mice: implications for Pierson syndrome.
Miner JH; Go G; Cunningham J; Patton BL; Jarad G
Development; 2006 Mar; 133(5):967-75. PubMed ID: 16452099
[TBL] [Abstract][Full Text] [Related]
20. A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.
Mohney BG; Pulido JS; Lindor NM; Hogan MC; Consugar MB; Peters J; Pankratz VS; Nasr SH; Smith SJ; Gloor J; Kubly V; Spencer D; Nielson R; Puffenberger EG; Strauss KA; Morton DH; Eldahdah L; Harris PC
Ophthalmology; 2011 Jun; 118(6):1137-44. PubMed ID: 21236492
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]